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dc.contributor.authorDemircan G.
dc.contributor.authorDiraman E.
dc.contributor.authorMiroglu Y.Y.
dc.contributor.authorDemircan S.
dc.contributor.authorYazici Z.
dc.contributor.authorCoban A.Y.
dc.contributor.authorYildirim T.
dc.contributor.authorBilir A.
dc.date.accessioned2019-09-01T12:50:11Z
dc.date.available2019-09-01T12:50:11Z
dc.date.issued2016
dc.identifier.issn1309-4483
dc.identifier.urihttps://dx.doi.org/10.5835/jecm.omu.33.03.002
dc.identifier.urihttps://hdl.handle.net/20.500.12450/583
dc.description.abstractIn this study, it was aimed to investigate that whether any change in activity of catalase (CAT), superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), lipid peroksidase and nitric oxide (NO) over time, and whether any difference between the different doses by giving different doses of aspirin to endothelial cells. Endothelial cells (HUVEC) in 24 wells microplates used in this study and 25, 50, 100, 250, 500, 750, 1000 and 1500 ?M aspirin to 2 of 4 wells at each row were given, the other 2 wells were included as controls. Accordingly, while CAT, SOD, GSH-Px levels and lipid peroxidation were being measured, NO release from cell media was observed. The significant differences were not found between the baseline (0 hour) CAT, SOD, GSH-Px and lipid peroxidase levels measured from lisates that obtained from the cells that different drug doses given and controls (p>0.05). Also, CAT, SOD, GSH-Px and lipid peroxidase levels at 24 (p>0.05), 48 and 72 hours did not show any difference among different drug doses and control (p>0.05). In the control group significant differences were found between CAT, SOD and GSH-Px levels measured at 0, 24, 48, 72 hours (p<0.05, p<0.05 and p<0.05 respectively) but lipid peroxidase activity and NO levels showed no difference. Increase in antioxidant enzyme activity in the cells that aspirin was not given, caused by raised free radical formation due to increase in number of cells by time was observed. Aspirin prevented the increase in reactive enzyme activity which increases by time. These results suggest that nontoxic doses of aspirin might protect the cells. © 2016 OMU.en_US
dc.language.isoengen_US
dc.publisherOndokuz Mayis Universitesien_US
dc.relation.isversionof10.5835/jecm.omu.33.03.002en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAspirinen_US
dc.subjectCell cultureen_US
dc.subjectEndotheliumen_US
dc.subjectNitrosative stressen_US
dc.subjectOxidative stressen_US
dc.titleEffects of aspirin on oxidative and nitrosative stress in vascular endothelial cell culturesen_US
dc.typearticleen_US
dc.relation.journalJournal of Experimental and Clinical Medicine (Turkey)en_US
dc.identifier.volume33en_US
dc.identifier.issue3en_US
dc.identifier.startpage129en_US
dc.identifier.endpage137en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.contributor.department-tempDemircan, G., Department of Medical Biology and Genetics, Faculty of Medicine, Istanbul Bilim University, Istanbul, Turkey -- Diraman, E., Department of Biology, Faculty of Science, Ondokuz Mayis University, Samsun, Turkey -- Miroglu, Y.Y., Ministry of National Education, Ordu, Turkey -- Demircan, S., Department of Cardiology, Faculty of Medicine, Istanbul Bilim University, Istanbul, Turkey -- Yazici, Z., Department of Virology, Faculty of Veterinary Medicine, Ondokuz Mayis University, Samsun, Turkey -- Coban, A.Y., Department of Microbiology, Faculty of Medicine, Ondokuz Mayis University, Samsun, Turkey -- Yildirim, T., Department of Biology, Faculty of Science, Amasya University, Amasya, Turkey -- Bilir, A., Department of Histology and Embryology, Faculty of Medicine, Zirve University, Gaziantep, Turkeyen_US


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